FDA label 55edceb9-4c87-df99-e063-6294a90a7962

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

SPL set ID: 55edceb9-4c86-df99-e063-6294a90a7962
SPL ID: 55edceb9-4c87-df99-e063-6294a90a7962
Version: 1
Effective date: 2026-07-06
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:07:57

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		55edceb9-4c87-df99-e063-6294a90a7962	id
spl set id		55edceb9-4c86-df99-e063-6294a90a7962	set_id

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For inhalation use only. Do not ingest or apply to skin. Use only in a well-ventilated area. Do not use in enclosed spaces. Avoid contact with eves. ears, and mouth. If product gets into eyes, rinse thoroughly with water for 15 minutes and seek medical help. May cause nasal irritation, coughing, or shortness of breath. Discontinue use if discomfort occurs and get fresh air immediately. Not recommended for individuals with: respiratory conditions (such as asthma or emphysema), heart disease, high blood pressure, or allergy to ammonia or strong odors.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.